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CD137 T细胞:免疫治疗革命的主角。

CD137 T-Cells: Protagonists of the Immunotherapy Revolution.

作者信息

Ugolini Alessio, Nuti Marianna

机构信息

Department of Experimental Medicine, "Sapienza" University of Rome, Viale Regina Elena, 324-00161 Rome, Italy.

Department of Immunology, H. Lee Moffitt Cancer Center, Tampa, FL 33612, USA.

出版信息

Cancers (Basel). 2021 Jan 26;13(3):456. doi: 10.3390/cancers13030456.

DOI:10.3390/cancers13030456
PMID:33530328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7866028/
Abstract

The CD137 receptor (4-1BB, TNF RSF9) is an activation induced molecule expressed by antigen-specific T-cells. The engagement with its ligand, CD137L, is capable of increasing T-cell survival, proliferation, and cytokine production. This allowed to identify the CD137 T-cells as the real tumor-specific activated T-cell population. In fact, these cells express various TCRs that are specific for a wide range of tumor-derived peptides, both shared and neoantigenic ones. Moreover, their prevalence in sites close to the tumor and their unicity in killing cancer cells both in vitro and in vivo, raised particular interest in studying their potential role in different strategies of immunotherapy. They indeed showed to be a reliable marker able to predict patient's outcome to immune-based therapies as well as monitor their response. In addition, the possibility of isolating and expanding this population, turned promising in order to generate effector antitumor T-cells in the context of adoptive T-cell therapies. CD137-targeting monoclonal antibodies have already shown their antitumor efficacy in cancer patients and a number of clinical trials are thus ongoing to test their possible introduction in different combination approaches of immunotherapy. Finally, the intracellular domain of the CD137 receptor was introduced in the anti-CD19 CAR-T cells that were approved by FDA for the treatment of pediatric B-cell leukemia and refractory B-cell lymphoma.

摘要

CD137受体(4-1BB,肿瘤坏死因子受体超家族9)是一种由抗原特异性T细胞表达的激活诱导分子。与它的配体CD137L结合能够增加T细胞的存活、增殖和细胞因子产生。这使得CD137 T细胞被确定为真正的肿瘤特异性激活T细胞群体。事实上,这些细胞表达多种TCR,它们对广泛的肿瘤衍生肽具有特异性,包括共享肽和新抗原肽。此外,它们在肿瘤附近部位的存在以及在体外和体内杀死癌细胞的独特性,引发了人们对研究它们在不同免疫治疗策略中潜在作用的特别兴趣。它们确实显示出是一种可靠的标志物,能够预测患者对基于免疫的治疗的结果以及监测他们的反应。此外,分离和扩增这个群体的可能性,在过继性T细胞治疗的背景下产生效应抗肿瘤T细胞方面变得很有前景。靶向CD137的单克隆抗体已经在癌症患者中显示出它们的抗肿瘤疗效,因此正在进行一些临床试验来测试它们可能引入不同免疫治疗联合方法中的情况。最后,CD137受体的胞内结构域被引入了经美国食品药品监督管理局批准用于治疗儿童B细胞白血病和难治性B细胞淋巴瘤的抗CD19嵌合抗原受体T细胞中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab1b/7866028/3f82d782d212/cancers-13-00456-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab1b/7866028/3f82d782d212/cancers-13-00456-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab1b/7866028/3f82d782d212/cancers-13-00456-g001.jpg

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